首页> 外文期刊>Vox Sanguinis: International Journal of Blood Transfusion and Immunohaematology >Influence of cell-free DNA in plasma on real-time polymerase chain reaction for determination of residual leucocytes in platelet concentrates.
【24h】

Influence of cell-free DNA in plasma on real-time polymerase chain reaction for determination of residual leucocytes in platelet concentrates.

机译:血浆中无细胞DNA对实时聚合酶链反应测定血小板浓缩物中残留白细胞的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND AND OBJECTIVES: Real-time quantitative (RQ) polymerase chain reaction (PCR) can be used to determine the number of residual leucocytes in leucocyte-reduced platelet concentrates (LR-PCs), which should contain < 3.3 leucocytes/ micro l. In this study we investigated the extent to which cell-free DNA, known to be present in plasma, might interfere with this determination. In this study, RQ-PCR was employed to determine the following: the influence of filtration of platelet concentrates (PCs) on the amount of cell-free DNA; the variation in concentration of cell-free DNA between the buffy coats (BCs) of different donors; and the amount of cell-free DNA during storage and processing of whole blood. MATERIALS AND METHODS: PCs were sampled before and after filtration (n = 5), BCs were sampled (n = 100) and whole blood units were sampled < 2 h and 16-20 h after collection, and the BCs were also sampled after processing the whole blood (n = 10). Samples were centrifuged to obtain cell-free plasma inwhich the amount of cell-free DNA was determined using an RQ-PCR for the albumin gene. RESULTS: The amount of cell-free DNA was not influenced by filtration of the PCs [1.7 +/- 0.8 vs. 1.5 +/- 0.8 leucocyte-equivalents (eq)/ micro l]. However, the amount of cell-free DNA in plasma of the BCs varied considerably, from 0.1 to 18.2 leucocyte-eq/ micro l (median = 1.5 leucocyte-eq/ micro l; mean +/- SD: 2.2 +/- 2.4 leucocyte-eq/ micro l). In 18% of the BCs the amount cell-free DNA was > 3.3 leucocyte-eq/ micro l. The amount of cell-free DNA increased during storage, from 0.3 +/- 0.3 leucocyte-eq/ micro l (< 2 h after collection) to 0.9 +/- 0.6 leucocyte-eq/ micro l (16-20 h after collection) and, after processing the whole blood, to 2.0 +/- 2.0 leucocyte-eq/ micro l. CONCLUSIONS: Variable amounts of cell-free DNA in plasma will interfere if RQ-PCR is applied to estimate leucocyte numbers in leucocyte-reduced PCs.
机译:背景与目的:实时定量(RQ)聚合酶链反应(PCR)可用于确定白细胞减少的血小板浓缩液(LR-PC)中的残留白细胞数量,该浓缩物中的白细胞含量应小于3.3微克/微升。在这项研究中,我们调查了血浆中已知存在的无细胞DNA可能干扰这一测定的程度。在这项研究中,RQ-PCR用于确定以下各项:血小板浓缩液(PC)过滤对无细胞DNA量的影响;不同供体的血沉棕黄层(BC)之间的无细胞DNA浓度变化;以及全血储存和加工过程中无细胞DNA的量。材料与方法:在过滤前后对PC进行采样(n = 5),对BCs进行采样(n = 100),并在采集后<2 h和16-20 h采样全血单位,并且在处理后还对BCs进行采样全血(n = 10)。离心样品以获得无细胞血浆,其中使用白蛋白基因的RQ-PCR确定无细胞DNA的量。结果:无细胞DNA的量不受PC过滤的影响[1.7 +/- 0.8对1.5 +/- 0.8白细胞当量(eq)/微升]。然而,BCs血浆中无细胞DNA的数量差异很大,从0.1到18.2白细胞当量/微升(中位数= 1.5白细胞当量/微升;平均值+/- SD:2.2 +/- 2.4白细胞-eq /微升)。在18%的BC中,无细胞DNA的量> 3.3白细胞当量/微升。储存过程中无细胞DNA的数量从0.3 +/- 0.3白细胞当量/微升(收集后<2小时)增加到0.9 +/- 0.6白细胞当量/微升(收集后16-20小时)在处理全血后,达到2.0 +/- 2.0白细胞当量/微升。结论:如果应用RQ-PCR估计白细胞减少的PCs中的白细胞数目,血浆中可变数量的无细胞DNA将受到干扰。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号